Background: Congenital Central Hypoventilation Syndrome (CCHS) is a rare genetic disorder causing alveolar hypoventilation due to impaired chemoreceptor response to hypercapnia and hypoxia due to a dysfunctional central autonomic drive. CCHS is a result of pathogenic variants of the PHOX2B gene which affects neural crest cell development. Consequently, CCHS can be accompanied with dysregulation of the autonomic system, Hirschsprung's disease and other gastrointestinal disorders, cardiac arrhythmias and neural cell derived tumors. Disease severity correlates with mutation type and determines ventilatory requirements, with management centered on lifelong respiratory support and multidisciplinary monitoring for associated comorbidities. Case Presentation: This case describes a term infant delivered via emergency cesarean section for maternal hypotension and fetal bradycardia who presented with apnea and required intubation due to failure to respond to positive pressure ventilation. The infant experienced recurrent apnea, hypercarbia, and ventilator dependence despite multiple failed extubation attempts, with an unrevealing evaluation for pulmonary, cardiac, neurologic, metabolic, and infectious causes. Genetic testing identified a PHOX2B polyalanine repeat expansion consistent with CCHS. This case demonstrates the stepwise multidisciplinary approach with concurrent genetic evaluation that enabled early diagnosis, timely management, and improved outcome.
Shalamov et al. (Thu,) studied this question.